> top > docs > PubMed:22898872 > annotations

PubMed:22898872 JSONTXT

Annnotations TAB JSON ListView MergeView

DisGeNET

Id Subject Object Predicate Lexical cue
T0 61-87 gene:7415 denotes valosin-containing protein
T1 20-23 disease:C0002736 denotes ALS
T2 166-321 gene:6647 denotes S) include, in addition to selective motor neuron (MN) degeneration, the occurrence of protein aggregates, mitochondrial dysfunction and astrogliosis. SOD1
T3 361-364 disease:C0002736 denotes ALS
T4 477-483 gene:23435 denotes TDP-43
T5 519-522 disease:C0002736 denotes ALS
T6 605-631 gene:7415 denotes valosin-containing protein
T7 773-779 disease:C1833662 denotes IBMPFD
T8 633-636 gene:7415 denotes VCP
T9 820-823 disease:C0002736 denotes ALS
T10 605-631 gene:7415 denotes valosin-containing protein
T11 663-678 disease:C0019247 denotes genetic disease
T12 605-631 gene:7415 denotes valosin-containing protein
T13 728-743 disease:C0005940 denotes disease of bone
T14 605-631 gene:7415 denotes valosin-containing protein
T15 748-771 disease:C0236642 denotes frontotemporal dementia
T16 605-631 gene:7415 denotes valosin-containing protein
T17 748-771 disease:C0338451 denotes frontotemporal dementia
T18 633-636 gene:7415 denotes VCP
T19 773-779 disease:C1833662 denotes IBMPFD
T20 605-631 gene:7415 denotes valosin-containing protein
T21 820-823 disease:C0002736 denotes ALS
T22 633-636 gene:7415 denotes VCP
T23 748-771 disease:C0338451 denotes frontotemporal dementia
T24 633-636 gene:7415 denotes VCP
T25 695-703 disease:C0026848 denotes Myopathy
T26 633-636 gene:7415 denotes VCP
T27 728-743 disease:C0005940 denotes disease of bone
T28 633-636 gene:7415 denotes VCP
T29 748-771 disease:C0236642 denotes frontotemporal dementia
T30 633-636 gene:7415 denotes VCP
T31 663-678 disease:C0019247 denotes genetic disease
T32 866-869 gene:7415 denotes VCP
T33 885-891 disease:C1833662 denotes IBMPFD
T34 893-896 gene:7415 denotes VCP
T35 885-891 disease:C1833662 denotes IBMPFD
R1 T0 T1 associated_with valosin-containing protein,ALS
R2 T2 T3 associated_with "S) include, in addition to selective motor neuron (MN) degeneration, the occurrence of protein aggregates, mitochondrial dysfunction and astrogliosis. SOD1",ALS
R3 T4 T5 associated_with TDP-43,ALS
R4 T6 T7 associated_with valosin-containing protein,IBMPFD
R5 T8 T9 associated_with VCP,ALS
R6 T10 T11 associated_with valosin-containing protein,genetic disease
R7 T12 T13 associated_with valosin-containing protein,disease of bone
R8 T14 T15 associated_with valosin-containing protein,frontotemporal dementia
R9 T16 T17 associated_with valosin-containing protein,frontotemporal dementia
R10 T18 T19 associated_with VCP,IBMPFD
R11 T20 T21 associated_with valosin-containing protein,ALS
R12 T22 T23 associated_with VCP,frontotemporal dementia
R13 T24 T25 associated_with VCP,Myopathy
R14 T26 T27 associated_with VCP,disease of bone
R15 T28 T29 associated_with VCP,frontotemporal dementia
R16 T30 T31 associated_with VCP,genetic disease
R17 T32 T33 associated_with VCP,IBMPFD
R18 T34 T35 associated_with VCP,IBMPFD

Allie

Id Subject Object Predicate Lexical cue
SS1_22898872_1_0 133-162 expanded denotes amyotrophic lateral sclerosis
SS2_22898872_1_0 164-167 abbr denotes ALS
SS1_22898872_1_1 203-215 expanded denotes motor neuron
SS2_22898872_1_1 217-219 abbr denotes MN
SS1_22898872_4_0 605-631 expanded denotes valosin-containing protein
SS2_22898872_4_0 633-636 abbr denotes VCP
AE1_22898872_1_0 SS1_22898872_1_0 SS2_22898872_1_0 abbreviatedTo amyotrophic lateral sclerosis,ALS
AE1_22898872_1_1 SS1_22898872_1_1 SS2_22898872_1_1 abbreviatedTo motor neuron,MN
AE1_22898872_4_0 SS1_22898872_4_0 SS2_22898872_4_0 abbreviatedTo valosin-containing protein,VCP

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 133-144 HP_0003202 denotes amyotrophic
T2 133-162 HP_0007354 denotes amyotrophic lateral sclerosis
T3 273-298 HP_0003287 denotes mitochondrial dysfunction
T4 273-286 HP_0001427 denotes mitochondrial
T5 695-703 HP_0003198 denotes Myopathy
T6 748-771 HP_0002145 denotes frontotemporal dementia
T7 763-771 HP_0000726 denotes dementia
T8 1155-1168 HP_0001427 denotes mitochondrial

DisGeNET5_variant_disease

Id Subject Object Predicate Lexical cue
22898872-5#55#60#geners121909329 897-902 geners121909329 denotes R155H
22898872-5#43#49#diseaseC1833662 885-891 diseaseC1833662 denotes IBMPFD
22898872-6#59#64#geners121909329 1046-1051 geners121909329 denotes R155H
22898872-6#37#41#diseaseC0035334 1024-1028 diseaseC0035334 denotes cord
55#60#geners12190932943#49#diseaseC1833662 22898872-5#55#60#geners121909329 22898872-5#43#49#diseaseC1833662 associated_with R155H,IBMPFD
59#64#geners12190932937#41#diseaseC0035334 22898872-6#59#64#geners121909329 22898872-6#37#41#diseaseC0035334 associated_with R155H,cord

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
22898872-0#61#87#gene7415 61-87 gene7415 denotes valosin-containing protein
22898872-0#20#23#diseaseC0002736 20-23 diseaseC0002736 denotes ALS
22898872-0#36#40#diseaseC0035334 36-40 diseaseC0035334 denotes cord
22898872-2#0#4#gene6647 317-321 gene6647 denotes SOD1
22898872-2#44#47#diseaseC0002736 361-364 diseaseC0002736 denotes ALS
22898872-3#55#61#gene23435 477-483 gene23435 denotes TDP-43
22898872-3#97#100#diseaseC0002736 519-522 diseaseC0002736 denotes ALS
22898872-4#32#58#gene7415 605-631 gene7415 denotes valosin-containing protein
22898872-4#60#63#gene7415 633-636 gene7415 denotes VCP
22898872-4#32#58#gene7415 605-631 gene7415 denotes valosin-containing protein
22898872-4#60#63#gene7415 633-636 gene7415 denotes VCP
22898872-4#175#198#diseaseC0236642 748-771 diseaseC0236642 denotes frontotemporal dementia
22898872-4#175#198#diseaseC0338451 748-771 diseaseC0338451 denotes frontotemporal dementia
22898872-4#175#198#diseaseC0236642 748-771 diseaseC0236642 denotes frontotemporal dementia
22898872-4#175#198#diseaseC0338451 748-771 diseaseC0338451 denotes frontotemporal dementia
22898872-4#147#170#diseaseC0029401 720-743 diseaseC0029401 denotes Paget's disease of bone
22898872-4#122#130#diseaseC0026848 695-703 diseaseC0026848 denotes Myopathy
22898872-4#147#170#diseaseC0029401 720-743 diseaseC0029401 denotes Paget's disease of bone
22898872-5#24#27#gene7415 866-869 gene7415 denotes VCP
22898872-5#51#54#gene7415 893-896 gene7415 denotes VCP
22898872-5#43#49#diseaseC1833662 885-891 diseaseC1833662 denotes IBMPFD
22898872-6#130#136#gene23435 1117-1123 gene23435 denotes TDP-43
22898872-6#37#41#diseaseC0035334 1024-1028 diseaseC0035334 denotes cord
61#87#gene741520#23#diseaseC0002736 22898872-0#61#87#gene7415 22898872-0#20#23#diseaseC0002736 associated_with valosin-containing protein,ALS
61#87#gene741536#40#diseaseC0035334 22898872-0#61#87#gene7415 22898872-0#36#40#diseaseC0035334 associated_with valosin-containing protein,cord
0#4#gene664744#47#diseaseC0002736 22898872-2#0#4#gene6647 22898872-2#44#47#diseaseC0002736 associated_with SOD1,ALS
55#61#gene2343597#100#diseaseC0002736 22898872-3#55#61#gene23435 22898872-3#97#100#diseaseC0002736 associated_with TDP-43,ALS
32#58#gene7415175#198#diseaseC0236642 22898872-4#32#58#gene7415 22898872-4#175#198#diseaseC0236642 associated_with valosin-containing protein,frontotemporal dementia
32#58#gene7415175#198#diseaseC0338451 22898872-4#32#58#gene7415 22898872-4#175#198#diseaseC0338451 associated_with valosin-containing protein,frontotemporal dementia
32#58#gene7415175#198#diseaseC0236642 22898872-4#32#58#gene7415 22898872-4#175#198#diseaseC0236642 associated_with valosin-containing protein,frontotemporal dementia
32#58#gene7415175#198#diseaseC0338451 22898872-4#32#58#gene7415 22898872-4#175#198#diseaseC0338451 associated_with valosin-containing protein,frontotemporal dementia
32#58#gene7415147#170#diseaseC0029401 22898872-4#32#58#gene7415 22898872-4#147#170#diseaseC0029401 associated_with valosin-containing protein,Paget's disease of bone
32#58#gene7415122#130#diseaseC0026848 22898872-4#32#58#gene7415 22898872-4#122#130#diseaseC0026848 associated_with valosin-containing protein,Myopathy
32#58#gene7415147#170#diseaseC0029401 22898872-4#32#58#gene7415 22898872-4#147#170#diseaseC0029401 associated_with valosin-containing protein,Paget's disease of bone
60#63#gene7415175#198#diseaseC0236642 22898872-4#60#63#gene7415 22898872-4#175#198#diseaseC0236642 associated_with VCP,frontotemporal dementia
60#63#gene7415175#198#diseaseC0338451 22898872-4#60#63#gene7415 22898872-4#175#198#diseaseC0338451 associated_with VCP,frontotemporal dementia
60#63#gene7415175#198#diseaseC0236642 22898872-4#60#63#gene7415 22898872-4#175#198#diseaseC0236642 associated_with VCP,frontotemporal dementia
60#63#gene7415175#198#diseaseC0338451 22898872-4#60#63#gene7415 22898872-4#175#198#diseaseC0338451 associated_with VCP,frontotemporal dementia
60#63#gene7415147#170#diseaseC0029401 22898872-4#60#63#gene7415 22898872-4#147#170#diseaseC0029401 associated_with VCP,Paget's disease of bone
60#63#gene7415122#130#diseaseC0026848 22898872-4#60#63#gene7415 22898872-4#122#130#diseaseC0026848 associated_with VCP,Myopathy
60#63#gene7415147#170#diseaseC0029401 22898872-4#60#63#gene7415 22898872-4#147#170#diseaseC0029401 associated_with VCP,Paget's disease of bone
32#58#gene7415175#198#diseaseC0236642 22898872-4#32#58#gene7415 22898872-4#175#198#diseaseC0236642 associated_with valosin-containing protein,frontotemporal dementia
32#58#gene7415175#198#diseaseC0338451 22898872-4#32#58#gene7415 22898872-4#175#198#diseaseC0338451 associated_with valosin-containing protein,frontotemporal dementia
32#58#gene7415175#198#diseaseC0236642 22898872-4#32#58#gene7415 22898872-4#175#198#diseaseC0236642 associated_with valosin-containing protein,frontotemporal dementia
32#58#gene7415175#198#diseaseC0338451 22898872-4#32#58#gene7415 22898872-4#175#198#diseaseC0338451 associated_with valosin-containing protein,frontotemporal dementia
32#58#gene7415147#170#diseaseC0029401 22898872-4#32#58#gene7415 22898872-4#147#170#diseaseC0029401 associated_with valosin-containing protein,Paget's disease of bone
32#58#gene7415122#130#diseaseC0026848 22898872-4#32#58#gene7415 22898872-4#122#130#diseaseC0026848 associated_with valosin-containing protein,Myopathy
32#58#gene7415147#170#diseaseC0029401 22898872-4#32#58#gene7415 22898872-4#147#170#diseaseC0029401 associated_with valosin-containing protein,Paget's disease of bone
60#63#gene7415175#198#diseaseC0236642 22898872-4#60#63#gene7415 22898872-4#175#198#diseaseC0236642 associated_with VCP,frontotemporal dementia
60#63#gene7415175#198#diseaseC0338451 22898872-4#60#63#gene7415 22898872-4#175#198#diseaseC0338451 associated_with VCP,frontotemporal dementia
60#63#gene7415175#198#diseaseC0236642 22898872-4#60#63#gene7415 22898872-4#175#198#diseaseC0236642 associated_with VCP,frontotemporal dementia
60#63#gene7415175#198#diseaseC0338451 22898872-4#60#63#gene7415 22898872-4#175#198#diseaseC0338451 associated_with VCP,frontotemporal dementia
60#63#gene7415147#170#diseaseC0029401 22898872-4#60#63#gene7415 22898872-4#147#170#diseaseC0029401 associated_with VCP,Paget's disease of bone
60#63#gene7415122#130#diseaseC0026848 22898872-4#60#63#gene7415 22898872-4#122#130#diseaseC0026848 associated_with VCP,Myopathy
60#63#gene7415147#170#diseaseC0029401 22898872-4#60#63#gene7415 22898872-4#147#170#diseaseC0029401 associated_with VCP,Paget's disease of bone
24#27#gene741543#49#diseaseC1833662 22898872-5#24#27#gene7415 22898872-5#43#49#diseaseC1833662 associated_with VCP,IBMPFD
51#54#gene741543#49#diseaseC1833662 22898872-5#51#54#gene7415 22898872-5#43#49#diseaseC1833662 associated_with VCP,IBMPFD
130#136#gene2343537#41#diseaseC0035334 22898872-6#130#136#gene23435 22898872-6#37#41#diseaseC0035334 associated_with TDP-43,cord